Synergistic blends of modified polyolefins and unmodified polyolefins

ABSTRACT

SYNERGISTIC EFFECTS IN CERTAIN PHYSICAL PROPERTIES HAVE BEEN FOUND IN BLENDS OF UNMODIFIED POLYOLEFINS WITH POLYOLEFINS WHICH HAVE BEEN MODIFIED BY REACTION WITH POLYMERIZABLE COMPOUNDS DEFINED BY   (CH2=C(-R2)-COO-R&#39;&#39;-)OXIRANE AND/OR   CH2=C(-R3)-(R4)(0-1)-SI(-R5)3   IN THE PRESENCE OF AN ORGANIC PEROXIDE. THE BLENDS ARE PARTICULARLY SUITABLE IN APPLICATIONS REQUIRING GOOD ADHESION TO POLAR SURFACES SUCH AS METAL AND GLASS.

United States Patent 3,696,069 SYNERGISTIC BLENDS 0F MODIFIED POLY- OLEFINS AND UNMODIFIED POLYOLEFINS Albert Schrage, East Orange, and Arnold B. Fiuestone, Woodclilf Lake, N.J., assignors to Dart Industries Inc., Los Angeles, Calif. No Drawing. Filed May 26, 1971, Ser. No. 147,187 Int. Cl. C08g 45/04 US. Cl. 260-41 R 9 Claims ABSTRACT OF THE DISCLOSURE Synergistic effects in certain physical properties have been found in blends of unmodified polyolefins with polyolefins which have been modified by reaction with polymerizable compounds defined by in the presence of an organic peroxide. The blends are particularly suitable in applications requiring good adhesion to polar surfaces such as metal and glass.

This invention relates to blends of modified polyolefin compositions and unmodified polyolefin compositions which exhibit synergistic efiects in certain physical properties such as adhesiveness characteristics.

Modified polyolefin compostiions having good adhesiveness characteristics, particularly toward polar materials, are described in copending applications Ser. No. 81,526, filed Oct. 16, 1970; Ser. No. 129,629 filed Mar. 30, 1971, entitled Modified Polyolefin Compositions Having Controlled Melt Flow (Schrage and Readio); and Ser. No. 129,623, filed Mar. 30, 1971 entitled The Use of Xylene in Controlling Melt Flow of Modified Polyolefin Compositions (Schrage and Readio). These compositions are formed, in general, by reacting an olefin polymer with certain ethylenically unsaturated polymerizable compounds in the presence of an organic peroxide. Certain acrylic esters of diols and triols or xylene may be included in the reaction mass if desired to control the melt flow of such modified polyolefin compositions. While these compositions do possess good adhesiveness characteristics and at the same time substantially retain their other physical properties they do involve the use of additional materials and processing steps as compared to unmodified polyolefin compositions and thus, for economic reasons, their use is limited to specialized applications rather than general purpose applications.

In accordance with this invention it was quite unexpectedly found that a blend of modified polyolefin compositions as described above with an unmodified polyolefin exhibits certain synergistic effects in adhesiveness characteristics. In general, the blends of the invention comprise from about 1% to 50% by weight. of the modified polyolefin composition and from about 50% to 99% by weight of the unmodified polyolefin although it would be expected that the synergistic effects would be obtained irrespective. of the relative proportions of the blend components.

The modified polyolefin compositions useful in the blends are those described in the aforementioned copending applications. These compositions are generally derived by reacting an olefin polymer and 0.01% to 10% by 3,696,069 Patented Oct. 3, 1972 weight based on the olefin polymer of a polymerizable compound defined by R is a cyclic, straight or branched chain alkylene group having 1 to 20 carbon atoms;

wherein R is a straight or branched chain alkylene radical having 1 to 10 carbon atoms, oxygen, sulfur, amino,

0 a u S- or wherein R is H or lower alkyl and R is lower alkyl;

wherein each R is a straight or branched chain lower alkylene, X is an amino group or an oxygen or sulfur atom, and p is an integer of 1 to 20;

r r l -CH1YR1 Y-CHaCHCH2-- L Jr:

wherein Y represents oxygen or sulfur atoms; R is a straight or branched chain alkylene radical having 1 to 10 carbon atoms,

oxygen, sulfur, or

wherein R is H or lower alkyl and R is lower alkyl; and n is an integer of l to 20;

wherein R is lower alkyl, x is an integer of 1 to 10 and z is an integer of l to 10;

wherein R is lower alkyl and r is an integer of l to 100;

wherein s is an integer of l to 100; and R is H or CH Preferably, R is a C -C alkylene group and R is H or CH By way of specific example of some of the compounds included in this definition there may be mentioned glycidyl acrylate; glycidyl methacrylate; the acrylic and methacrylic esters of the monoglycidyl ether of sulfonyl bis-phenol, the monoglycidyl ether of a C to C alkylene bisphenol, the monoglycidyl ether of oxybisphenol, the monoglycidyl ether of thiobisphenol, the monoglycidyl ether of aminobisphenol and the monoglycidyl ether of a,u-bis(p-hydroxyphenyl) tolylethane; the acrylic and methacrylic esters of 3-oxy-6,7-epoxyhaptanol; the reaction products of one mole of acrylic or methacrylic acid with one mole of polyphenylenesulfide diglycidyl ether, polyphenyleneamine diglycidyl ether, or polyphenyleneoxide diglycidyl ether; the reaction products of one mole of acrylic acid or methacrylic acid with one mole of the polycondensation product of epichlorohydrin with sulfonyl bis(phenylmercaptan) or sulfonyl bisphen01; the reaction products of one mole of acrylic acid or methacrylic acid with one mole of the polycondensation product of epichlorohydrin with a,a-bis(p-hydroxyphenyl) tolylethane or a,a,-bis(p-thiophenyl)tolylethane; the acrylic and methacrylic esters of poly (C -C alkyleneoxide glycol) monoglycidyl ether; and the acrylic and methacrylic esters of poly [(co-alkylene-phenylene-oxide) glycol] monoglycidyl ether. All of these compounds are disclosed in copending application Ser. No. 81,527 filed Oct. 16, 1970.

Also included within the polymerizable compounds are those compounds defined by wherein R is hydrogen or an alkyl radical having 1 to 4 carbon atoms;

R is a straight, branched or cyclic alkylene radical having 1 to 10 carbon atoms with or without pendant glycidoxy groups; a substituted or unsubstituted phenylene group with or without pendant glycidoxy groups;

with or without pendant glycidoxy groups;

a O-(C Cm a1kylene)- group with or without pendant glycidoxy groups; or

0 a -(Cr-C1o alkylene)gO(Ci-Cm alkylene) group with or without pendant glycidoxy groups; and R is halogen (bromine or chlorine in particular), an alkoxy radical having 1 to carbon atoms, or an acyloxy radical having 1 to 10 carbon atoms.

Preferably, R is absent or a C -C alkylene group while R and R are as described above.

Included within the above defined group of compounds are the following by structure onmnQ-suoonm Such compounds are commercially available.

The above olefin polymer and polymerizable compound are reacted in the presence of an organic peroxide, preferably 0.01% to 5% by weight based on the olefin polymer. Suitable organic peroxides useful in this invention include both solid and liquid organic peroxides. In order to insure good distribution of the peroxide throughout the mixture of ingredients prior to reaction it is preferred to use a liquid form of the peroxide. Thus, for convenience, those organic peroxides which are normally liquid or which become liquid at or near the temperature at which the particular reaction is run are preferred over the solidtype organic peroxides. However, by dissolving the solid organic peroxides in a suitable organic solvent, that is one that has no substantial adverse effect on free radical polymerization reactions, a suitable physical form is obtained which can be used with substantially equal success in the process of the invention. Since the solvent, for this purpose, merely functions as a carrier for the solid organic peroxide it makes no difference whether or not it becomes vaporized prior to teaching reaction temperature since the peroxide at that point in the process has already been distributed throughout the ingredients.

Some examples of suitable peroxides include di-t-butyl peroxide, t-butyl hydroperoxide, methyl ethyl ketone peroxide, t-butyl perbenzoatc, t-butyl peracetate, t-butyl peroxypivalate, acetyl peroxide, t-butyl peroctoate, t-butyl peroxyisobutyrate, decanoyl peroxide, lauroyl peroxide, benzoyl peroxide, 2,5-dimehylhexane-2,5-diperoxybenzoate, cyclohexanone peroxide, cumene hydroperoxide, p-methane hydroperoxide, di t butyl-diperoxyphthalate, cumyl peroxide, caproyl peroxide, and the like. Of course, there are additional organic peroxides in this group but are too numerous to attempt to individually name. In the event it is desirable to use a solvent some which would be suitable include benzene, mineral spirits, toluene, chlorobenzene, dichlorobenzene, acetone, dimethyl phthalate, t-butyl alcohol, anisole, decalin, xylene and others which possess the required inertness to the reaction. The use of xylene for this purpose also offers additional advantages in the reaction in that it functions to control the melt flow of the resulting composition, all of which is described later herein. As mentioned previously, it is preferred that the organic peroxide be in a liquid form or capable of dissolution in a substantially inert organic solvent at or near the temperature at which the particular reaction is carried out.

It is pointed out that oxygen cannot be employed in the process even though it is sometimes regarded as a free radical initiator. Oxygen is known to cause deleterious effects on polymerizable monomers such as the ethylenically unsaturated compounds and acrylic esters used in this invention (see page 36 of the reprint of Chapters I-IV from Monomeric Acrylic Esters by E. H. Riddle, 1954).

Selection of a particular organic peroxide or mixture of organic peroxides of the type mentioned above may be easily determined based on the temperature at which the particular reaction is to be carried out and the corresponding decomposition rate of the peroxides as evidenced by their respective half-lives. The half-lives of peroxides are well known and may be readily ascertained (see US. 3,293,233 and Encyclopedia of Chemical Technology, Kirk-Othmer, 2d edition, vol. 14, pp. 810-813).

Optionally, for melt flow control purposes, either xylene or an acrylic ester of a diol or triol or mixtures thereof may be employed in the reaction mass and subjected to reaction conditions along with the olefin polymer and polymerizable compound. The melt fiow control eifect achieved with the use of these modifiers in the reaction is one of lowering the melt flow. Thus, without the use of these modifiers the modified polyolefin compositions tend to have rather high melt flow values whereas when these modifiers are employed in the reaction the melt flow values of the modified compositions are significantly lower. All of this is described in the aforementioned copending applications Ser. Nos. 129,623 and The acrylic esters of diols or triols which may be used as the modifier in the invention include those defined by the following formula wherein R is defined above and R is H or crr R wherein R is defined above; R for each unit is H or ---CH;.,; and

The above acrylic esters are either commercially available or may be prepared by conventional direct esterification techniques involving reaction between acrylic acid or methacrylic acid and the particular diol or triol. Conventional acylation techniques may also be used wherein acryloyl chloride or methacryloyl chloride are substituted for the acids in reacting with the diols or triols.'

Any diol or triol coming within the scope of the corresponding portion of the above structural formula may be used for such preparation. For example, ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, dipropylene glycol, polypropylene glycols, hexylene glycol, 2-methyl-2-ethyl-1,3-propanediol, 2- ethyl-l,3-hexanediol, 1,5-pentanediol, glycerin, 1,2,6- hexanetriol, triethanol amine, diethanol amine, 1,4-butanediol, polyethylene glycol, 1,2,4-hexanetriol, trimethylol ethane, trimethylol propane, poly(oxypropylene)poly (oxyethylene) glycols and alkylene triols, poly(oxypropyleneoxyethylene) glycols and alkylene triols, and the like.

The preferred acrylic esters are those defined by the formula u IW-JJ-O-R l gxs R J0-R" wherein each R is H or --CH R is 2)o-1 -R ]o-1 wherein R is H or C -C alkyl; and R is o R =CHz wherein R is H or CH The manner in which the materials are reacted is not critical. Thus, for example, it may be expeditious to merely admix the materials using any type of mixing device and, after charging the mixture to a reactor, heating the mixture to an optimum temperature Whereat the organic peroxide decomposes to generate free radicals. The reaction may be conducted with all of the ingredients dissolved in inert solvents or while in a molten state. Or the olefin polymer may be molten or in solid particulate form while the remaining ingredients are in a liquid or dissolved state.

The temperature is also not critical for conducting the reaction except to the extent that it must not be so high as to cause degradation of the olefin polymer, the ethylenically unsaturated compound, or the acrylic esters. As mentioned above, the temperatures employed go hand-inhand with the particular peroxide selected. For example, if it is desired to conduct the reaction at a low temperature one would most likely select a peroxide having a low temperature 10-hr. half-life, e.g. acetyl peroxide for use at about room temperature.

The pressure at which the reaction is conducted is not critical and, in general, good results can be obtained at pressures in the range of atmospheric up to about 1000 p.s.i. For practical reasons it is convenient to operate at pressures of atmospheric up to about 200 p.s.i.

Since oxygen has some adverse effect on the reaction it is desirable to conduct the reaction in a substantially oxygen-free atmosphere if possible. While small amounts of oxygen can probably be tolerated in the system eifort should be made to prevent introduction of additional oxygen over and above what may be initially present. Preferably, the reactor is purged with an inert gas prior to conducting the reaction.

In conducting the reaction using a solid form of polyolefin it is desirable to substantially completely decompose the organic peroxide before recovering the product as the presence of any residual peroxide, even in small quantities, may adversely afiect'the resulting composition in subsequent compounding, molding or extruding opera tions. Of course, if one can tolerate certain of the adverse effects then the extent of decomposition of the peroxide may be somewhat incomplete.

As mentioned previously the blends of this invention are formed by blending the above modified polyolefin composition, generally from 1% to 50% by weight, preferably 1% to 20% by weight, with an unmodified polyolefin composition, generally from 50%to 99% by weight.

The unmodified polyolefin may include any olefin polymer derived from alpha-olefin monomers having 2 to 10 carbon atoms such as polyethylene, polypropylene, poly butene-l poly (4-methyl pentene- 1 ethylene-propylene 8 with stirring under autogenous pressure and maintaining that temperature for about four hours. After cooling, the modified polypropylene composition was recovered in a particulate form.

random and block copolymers and z g a gg In order to demonstrate the synergistic adhesiveness char- 'p p ii 1- g f s :8 a: are g acteristics of the blend, samples of the blend and the modibe 0 e n 2.? g fi g mono fied polypropylene composition were each reinforced with mmfied. W r g 01 met of the 20% by weight chopped glass fibers A inchO( ?F 885) met .whlch 3 Presen .5. e o p y using conventional extrusion techniques. Each reinforced modlfied Po yo 6 5 g merel h sican tumbl sample was then molded into test specimens and tested for The blends may 6 (mm 2' y o y onents fiexural strength and modulus in accordance with ASTM mg i q g gg gi g fi gi5 2 gg g g D-790-66. The results are indicated in the following may 6 m e 51% y table along with the average typical results obtained from roll mill or an extruder. identical testin f g 0 several samples of polypropylene (un- Various additives may be incorporated into the blends, 5 modified) reinforced with b Wei ght glass fibers or one or the other component, or both cQ P 'E (V4 ocp 5) y Such additives include fillers, stabilizers, antioxidants, slip agents, anti-static agents, mold release agents, flame re- TABLE 1 tardants, pigments and the like. Flexuml The blends of this invention exhibit certain 1synergistic 20 g gl g i adhesiveness characteristics and are particular y suita y 1 s rengi .s. for producing fiber reinforced compositions, e.g bleigds Compositm with 20%gass fibers (D- 800) containing 5% to 90% glass fibers, and coat ngs 0r 10,000 various substrates, e.g. metal surfaces such as the In ri r g ggl poiypmmlene of metallic containers. Predicted 0010-5 The synergistic adhesiveness properties f e blelids Actualuml; i "I I 1:500 tb 1 are demonstrated by the adhesion of the blends to rein- 1Blend p mm y we ghtpo yp py one an va y s forcing glass fibers as indicated y flexural Strength a modified polypropylene composition in accordance with this nvent on. modulus preperties of molded test specimens of such rein- EXAMPLE 2 forced blends. The following examples serve to illustrate this synergism A ser1es of blends in accordance with the invention EXAMPLE 1 were prepared employing modified polypropylene comd I positions each of which was derived from 100 parts by A blend "t accorfipce was Pm weight powder polypropylene and varying amounts of pared by physcauy mlxmg the 0 lowmg glycidyl acrylate in the presence of 0.5 part by weight (A) 9 parts by weight polypropylene powder and t-butyl peracetate. The modified polypropylene composi- (B) 1 part by weight of a modified polypropylene comtions were prepared as in Example 1 except that the reposition prepared by reacting 100 parts by weight polyaction was conducted in a continuously rotated l-liter propylene powder and 1.5 parts by weight glycidyl flask partially immersed inaconstant temperature oil bath acrylate in the presence of 0.5 part by weight t-butyl 40 (125 C.) for about four hours. The several blends and peracetate solution in benzene). The preparacorresponding modified polypropylene compositions were tion comprised mixing the ingredients in a Waring reinforced with 20% by weight glass fibers and tested in blender, charging them to a purged reactor equipped the same manner as described in Example 1. The results with a stirrer followed by heating to about C. are indicated in the following table.

TABLE 2 Composition Glyeldyl Weight ratio 0t with 20% acrylate PP to MPP in blend Flexural glass fibers (parts by Fiexurel modulus (PP, MPP, weight strength .s.i.) Series N o. blend) in MPP) (p.s.i.) (X106) Control PP 10, 000 4. 9 gggg C Blend 9/1 {Predictedu ca. 10,500 ca. +4. 9

1263s a; c ua Blend 9/1 {Predictei ca. 10,500 ca. -4.9

{i188 C 118 Blend 9/1 {Predieted ca. 10,500 ca. +4.9

D MPP 55% it 11 Blend {Pi edi cmm ca.10,500 68.+4.9

E MPP 2.0 14, 500 4.5

9/1 {Aetualun 13,600 5/- Predicted. ca. 10, 500 ca. 4. 9

2.0 1a, 900 4 5 9/1 {Actual. 13,800 5.1 Predicted. ,400 ca. -4. 9

3.0 15, 600 5.2 9/1 Actualnu' 14,800 5.0 Predi tedca. 10,600 ca. +4.9 Actual 14,700 5.2 Predlcted. ca. 10, 400 ca. +4. 9 19/1 {Act1111 14 00 5.3 Predicted. ca. 10,300 ca. +4.9

Nora.PP=Polypi-opylene,

EXAMPLE 3 TABLE 3 Flexural Flexural modulus strength (p.s.i.)

Composition with 20% glass fibers (p.s.i.) (X10 Polypropylene 10, 000 4. 9

Modified block copolymer 3. 6 Blendz Actual 12, 700 3. 8

Predicted ca. 10,400 ca 4. 8

l Blend comprises 9/1 weight ratio of polypropylene to modified block copolymer.

EXAMPLE 4 A blend in accordance with the invention was prepared and tested as in Example 3 except that a modified polypropylene composition was blended with a block copolymer of propylene and ethylene. The modified polypropylene composition was prepared using 100 parts by weight polypropylene, 3 parts by weight glycidyl acrylate and 0.5 part by weight t-butyl peracetate. The results of the tests appear in the following table.

TABLE 4 Flexural Flexural modulus strength (p.s.i.)

Composition with 20% glass fibers (p.s.i.) (X 10 Block copolymer of propylene and ethylene..-. 8, 700 4. 6

Modified polypropylene 15, 100 4. 5 Blend: 1

ca. 9,400 ca. 4. 6

Blend comprises 9/1 weight ratio of block copolymer of propylene and ethylene with modified polypropylene composition.

EXAMPLE 5 A blend in accordance with the invention was prepared and tested as in Example 3 except that a modified polypropylene composition was blended with an unmodified polypropylene. The modified polypropylene composition was prepared using 100 parts by weight polypropylene, 2 parts by weight 'y-methacryloxypropyl trimethoxy silane and 0.5 part by weight t-butyl peracetate. The results of the tests appear in the following table.

TABLE 5 Flexural Flexural modulus strength (p.s.i.)

Composition with 20% glass fibers (p.s.i.) (X10 Polypropylene 10, 000 4. 9

Modified polypropylene 16, 500 5. 0 Blend: 1

Actual 15, 400 5. 0

Predicted ca. 10, 700 ca. +4. 9

Blend comprises 9/1 weight ratio of polypropylene with modified polypropylene composition.

EXAMPLE 6 TABLE 6 Flexural Flexural modulus strength (p.s.i.)

Composition with 20% glass fibers (p.s.i.) (X 10 Polypropylene 10, 000 4. 9

Modified polypropylene- 14, 600 4. 6 Blend: 1

Actual- 14,300 4. 9

Predicted ca. 10,500 ca. 4.9

Blend comprises 9/1 weight ratio of polypropylene with modified polypropylene composition.

EXAMPLE 7 A blend in accordance with the invention was prepared and tested in a manner similar to that described in Example 2 except that the modified polyolefin composition was prepared from parts by weight polypropylene, 1.5 parts by weight glycidyl acrylate, and 1.0 part by weight ethylene glycol dimethacrylate in the presence of 0.5 part by weight t-butyl peracetate. The blend was prepared from the above modified polypropylene composition and unmodified polypropylene. The test results are shown in the following table.

TABLE 7 Flexural Flexural modulus strength (p.s.i.) Composition with 20% glass fibers (p.s.i.) (X10 Polypropylene 10, 000 4. 9 Mlodlgied polypropylene 15, 500 5. 1

Actual 14, 600 5. 0 Predicted 10, 600 +4. 9

Blend comprises 9/1 weight ratio of polypropylene and modified polypropylene composition.

EXAMPLE 8 A blend in accordance with the invention was prepared and tested as in Example 5 except that the blend was a 1/1 weight ratio of modified polypropylene composition with unmodified polypropylene. The modified polypropylene was prepared using 100 parts by weight polypropylene powder, 2 parts by weight glycidyl acrylate, and 0.75 part by weight t-butyl peracetate. The results of the tests appear in the following table.

Thus having described the invention in detail it will be understood by those skilled in the art that certain variations and modifications may be made without departing from the spirit and scope of the invention as described herein or in the appended claims.

We claim:

1. A blend comprising (1) from about 5-0 to about 99 percent by weight of an olefin polymer derived from alpha-olefin monomers having 2 to 10 carbon atoms and (2) from about 1 to about 50 percent by weight of a reaction product of (A) at least one olefin polymer derived from alphaolefin monomers having 2 to 10 carbon atoms, and

(B) from about 0.01 to 10 percent by weight of the olefin polymer of at least one polymerizable compound defined by 1 1 1 2 wherein 4. A blend according to claim 1 wherein the reaction R is a cyclic, straight or branched chain alkylproduct includes, in addition to (A) and (B), (C) at ene group having 1 to 20 carbon atoms; least one modifier defined by the formula wherein R is a straight or branched chain iw Ho alkylene radical having to 10 carbon atoms, oxygen, sulfur, amlno, k 0-40 if wherein e each R is H or C -C alkyl;

R is 01' I lcnn l.

R1 15 /o4o wherein R is H or C -C alkyl; n 0 o lo Rs 0-40 20 wherein R is defined above;

wherein R" is H or lower alkyl and R is ficRwrlf T lower alkyl; 0-1

1 wherein R is defined above and R is H or aR-X-R group L J leg l Rla wherein each R is a straight or branched /1-: chain lower alkylene, X is an amino group or or an oxygen or sulfur atom, and p ls an l integer of 1 to 20;

wherein Y represents oxygen or sulfur wherein R is defined above; atoms, R is a straight or branched chain R for each unlt 1s H or -CH and alkylene radical having 1 to .10 carbon R is atoms, 0 321 (III) -E-=CHg s wherein R is H or CH;,.

5. A blend according to claim 1 wherein the reaction oxygen sulfur or product is derived from (A) and (B) in the presence of xylene in addition to the organic peroxide.

I 6. A blend according to claim 1 wherein the polymerizable compound is defined by O O R wherein R11 is H or lower alkyl and R12 is whceillein R is a C -C alkylene group and R is H or lower alkyl; and n 18 an Integer 5. to 20; 7. A blend according to claim 1 containing 5% to 90% by weight reinforcing fibers.

a a L Q QJ. gmup s. A metallic article coated with the blend of claim 1.

h i 13 i lower alkyl, x is an integer 9. A blend according to claim 1 wherein the olefin polyf 1 to 10 and z is an integer f 1 to 10; mer of (1) is polypropylene, polyethylene, or a copoly- 0 mer of ethylene and propylene; the reaction product of a CHz 0R group (2) is derived from (A) polypropylene, polyethylene, or

L a copolymer of ethylene and propylene, (B) a polymerwherein R is lower alkyl and r is an inizable compound which is glycidyl acrylate or glycidyl tegel' 0f 1 t0 methacrylate, and, optionally, (C) a modifier which is ethylene glycol diacrylate, ethylene glycol dimethacrylate, a trimethylol propane triacrylate, trimethylol propane tri- 0 methacrylate 1,3-butylene diacrylate, or 1,3-butylene difg fl g c $1 an lmeg of 1 to 1003 and R2 methacrylate: in the presence of an organic peroxide. 1 3. 2. A blend according to claim 1 wherein the olefin poly- 7 R f e Cited mer of the reaction product 18 polypropylene, polyethyl- UNITED STATES PATENTS ene, or a copolymer of ethylene and propylene.

3. A blend according to claim 1 wherein the olefin poly- 3322661 5/1967 Yoshlkavia 204159 mer of (1) is polypropylene, polyethylene or a copolymer 3179485 4/1965 Kawasakl 204 159-17 of propylene and ethylene. (Other references on following page) 13 FOREIGN PATENTS 1,038,726 8/ 1966 Great Britain 260-857 3,713,880 9/1962 Japan. 4,218,327 9/1967 Japan. 4,316,392 7/ 19-68 Japan. 4,328,461 12/1968 Japan. 447,345 3/1969 Japan.

OTHER REFERENCES 14 Methacrylate Onto Polypropylene and Polyvinyl Chloride F)ibers; Bull Chem. Soc. Japan, 38(8) 1349-1354 (1965 Chemical Abstracts: vol. 59, p. 77220 (1963); vol. 68, p. 22496); (1968); vol. 70, p. 5884-6s (1969); vol. 70, p. 79086j (1969); vol. 71, p. 22877j (1969); vol. 71, p. 22878k (1969); vol. 71, p. 22879m (1969); vol. 71, p. 14138d (1969).

PAUL LIEBERMAN, Primary Examiner US. Cl. X.R.

117-l23 D, 132 C, BE, BS; 260-37 Ep, 41 Ag, 94.7 A, 827, 878 R, 836

1 PM 5 Dam October 3., '1972' inventor) Albert Sohrage and "Arnold B. Finestone It is certified that error appears in the above-identified patent and that said Letters. Patent are hereby corrected as shown below:

Column 11, Q lines 32-35, that portion of the formula reading CH2-EY -CH EY Column 11, lines 55-57, that portion of the formula reading should read -CH I should read vCH Column 11, lines 65-67, that portion of the formula reading CH should read -CH Column ll, line 69 after ."CH3" add in the presence of an organic peroxide v Signed and sealed this 8th dayof May 1973.

(SLAL) Attest:

ROBERT GOTTSCHALK Commissioner of Patents LIDK'JARD i-LFLETCHERQTL Attesting Officer 

